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HRID 256605作成日:2026年10月26日

Triethylamine → N-(2-Chloro-4-methylphenyl)methanesulfonamide

https://huagongshe.com/reaction/256605

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2-Chloro-p-toluidineHCID 12007—
反応物Methanesulfonyl chlorideHCID 31297—
溶媒DichloromethaneHCID 6344—
生成物N-(2-Chloro-4-methylphenyl)methanesulfonamideHCID 1978560932.3%

反応手順

A solution of 2-chloro-4-methylaniline (5.00 g) and triethylamine (3.57 g) in dichloromethane (100 ml) was cooled to 0° C. Methanesulphonyl chloride (4.04 g) was added dropwise and the mixture stirred at ambient temperature overnight. The mixture was then washed with 2N aqueous hydrochloric acid solution (50 ml) and the solvent removed by evaporation. The residue was dissolved in ethyl acetate (75 ml) extracted with 2N aqueous sodium hydroxide solution (2×50 ml). The aqueous phase was acidified with 2N aqueous hydrochloric acid solution and extracted with ethyl acetate (2×75 ml). This was subsequently dried (MgSO4) and the solvent evaporated. Thus was obtained N-(2-chloro-4-methylphenyl)methanesulphonamide (2.5 g, 32%). NMR Spectrum 2.33 (3H, s), 2.97 (3H, s), 6.6 (1H, s), 7.10 (1H, d), 7.25 (1H, s), 7.52 (1H, d).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05258399
出典データセットuspto-grants-1993_11
ORD IDord-0533d51cf27c41d48af9351d24ce8f58
出典メモuspto-grants-1993_11